Dentifrice Compositions With Improved Fluoride Uptake

ABSTRACT

Certain alkaline dentifrice compositions with relatively high level of water and calcium-containing abrasive, a basic amino acid, and a relatively low level of humectant, have a surprisingly high fluoride uptake.

FIELD OF THE INVENTION

The present invention relates to dentifrice compositions having a basic amino acid and a fluoride ion source, have improved fluoride uptake.

BACKGROUND OF THE INVENTION

Dentifrice compositions are well known for dental and oral hygiene care. High water (e.g., >44 wt %) and high carbonate (e.g., >24 wt %) formulation chassis are cost effective for many markets and consumers. Dental plaque is a sticky, colorless deposit of bacteria that is constantly forming on the tooth surface. Saliva, food and fluids combine to produce these deposits that collect where the teeth and gums meet. Plaque buildup is the primary factor in poor oral health that can lead to caries and periodontal (gum) disease, including gingivitis. One way dentifrice compositions help prevent and control plaque is by leveraging anti-bacterial agents; however, the disadvantage and formulation challenge is the unintended reactivity of anti-bacterial agents with formulation ingredients and environment of containing calcium carbonate matrix. This may include oxidative degradation, hydrolysis, adsorption or precipitation of oxy-hydroxide species, any of which can impact the bio-availability of the anti-bacterial agent. There is a continuing need to provide such formulations that help prevent plaque formation on teeth and/or minimize the use of antimicrobial agents, particularly in high water and high carbonate dentifrice formulation chassis.

Fluoride ion sources, such as sodium monofluorophosphate, are well known for their anti-caries benefit. Fluoride uptake in dental plaque is an important metric in assessing the efficacy of anti-plaque or plaque mitigation benefits of the dentifrice compositions described herein. Fluoride is known to have the potential to exert an anti-caries benefit largely through three mechanisms; inhibition of demineralization, promotion of remineralization and interference with bacterial growth and metabolism. Small but protracted elevations in fluoride levels are linked to modification of the demineralization/remineralization balance by direct effects on the dental mineral. Plaque fluoride levels have been clinically correlated with dose response in providing anti-caries. Thus the fluoride pharmacokinetic reservoirs and the bioavailability of fluoride in saliva, and consequently in plaque fluid, play a crucial role in preventing a net mineral deficit. The source of the fluoride can also play an important role as the source used will lead to different salivary fluoride concentrations post brushing. Sodium monofluorophosphate (Na-MFP) requires hydrolysis to release free fluoride ions. The different dissolution properties can lead to different fluoride concentrations in plaque, consequently affecting the caries protective effect of plaque fluoride content. The fluoride binding to the plaque reservoirs and the release from the reservoir is a complex multi-mechanism; binding to the anionic sites on the bacterial wall, within the plaque matrix constituents via calcium bridging, binding to calcification nuclei or diffusion kinetics based on the specific plaque matrix.

Basic amino acids, such as arginine bicarbonate, are well known for their benefits combating cavity formation, and/or tooth sensitivity; and/or providing pH neutralizing effects.

However, at least some commercialized dentifrice products having arginine bicarbonate have less than optimized fluoride uptake. Accordingly there is a need to for high water (e.g., >44 wt %), high carbonate (e.g., >24 wt %), fluoride ion source, basic amino acid containing dentifrice compositions having improved fluoride uptake in dental plaque.

SUMMARY OF THE INVENTION

A surprising discovery is the negative influence of higher levels of sorbitol/glycerol in fluoride uptake in dental plaque in high water, high carbonate, fluoride ion source, and basic amino acid containing dentifrice formulations. Reduced levels of sorbitol/glycerol in these dentifrice compositions provide superior fluoride uptake results.

One aspect of the invention provides for a dentifrice composition comprising: 45% to 75%, by weight of the composition, of water; 25% to 50%, by weight of the composition, of a calcium-containing abrasive (e.g., calcium carbonate); 0.0025% to 2%, by weight of the composition, of a fluoride ion source (e.g., sodium monofluorophosphate); 0.0025% to less than 7%, by weight of the composition, of a basic amino acid in free or salt form (e.g., arginine bicarbonate (in acid or salt form); 0% to 10%, by weight of the composition, of a humectant, wherein the humectant is selected from sorbitol, glycerol, and combination thereof; and wherein said composition has a pH greater than 7.8.

Another aspect of the invention provides for a dentifrice composition comprising: 45% to 75%, by weight of the composition, of water; 25% to 50%, by weight of the composition, of a calcium carbonate; 0.1% to 2%, by weight of the composition, of a sodium monofluorophosphate; 0.1% to less than 7%, by weight of the composition, of arginine bicarbonate; (e) 0% to 5%, by weight of the composition, of a humectant; wherein said composition has pH from 8.5 to 10.5; and said composition is a single phase composition.

Yet another aspect of the invention provides a method of treating tooth enamel comprising the step of brushing teeth with a dentifrice composition of the present invention.

Yet still another aspect of the invention provides a method preventing or mitigating plaque formation on tooth enamel comprising the step of brushing teeth with a dentifrice composition of the present invention.

These and other features, aspects, and advantages of the present invention will become evident to those skilled in the art from the detailed description which follows.

DETAILED DESCRIPTION OF THE INVENTION Definitions

The term “comprising” as used herein means that steps and ingredients other than those specifically mentioned can be added. This term encompasses the terms “consisting of” and “consisting essentially of.” The compositions of the present invention can comprise, consist of, and consist essentially of the essential elements and limitations of the invention described herein, as well as any of the additional or optional ingredients, components, steps, or limitations described herein.

The term “dentifrice” as used herein means paste, gel, powder, tablets, or liquid formulations, unless otherwise specified, that are used to clean the surfaces of the oral cavity. Preferably the dentifrice compositions of the present invention are single phase compositions. The term “teeth” as used herein refers to natural teeth as well as artificial teeth or dental prosthesis.

All percentages, parts and ratios are based upon the total weight of the compositions of the present invention, unless otherwise specified. All such weights as they pertain to listed ingredients are based on the active level and, therefore do not include solvents or by-products that may be included in commercially available materials, unless otherwise specified. The term “weight percent” may be denoted as “wt %” herein. All molecular weights as used herein are weight average molecular weights expressed as grams/mole, unless otherwise specified.

As used herein, the articles including “a” and “an” when used in a claim, are understood to mean one or more of what is claimed or described.

As used herein, the terms “comprise”, “comprises”, “comprising”, “include”, “includes”, “including”, “contain”, “contains”, and “containing” are meant to be non-limiting, i.e., other steps and other sections which do not affect the end of result can be added. The above terms encompass the terms “consisting of” and “consisting essentially of”.

As used herein, the words “preferred”, “preferably” and variants refer to embodiments of the invention that afford certain benefits, under certain circumstances. However, other embodiments may also be preferred, under the same or other circumstances. Furthermore, the recitation of one or more preferred embodiments does not imply that other embodiments are not useful, and is not intended to exclude other embodiments from the scope of the invention.

Water

The dentifrice compositions of the present invention comprise herein from 45% to 75%, by weight of the composition, of water. Preferably, the dentifrice composition comprises from 45% to 65%, more preferably from 45% to 55%, yet more preferably from 46% to 54%, by weight of the composition, of water. The water may be added to the formulation and/or may come into the composition from the inclusion of other ingredients. Preferably the water is USP water.

Calcium-Containing Abrasive

The compositions of the present invention comprise from 25% to 50%, by weight of the composition, of a calcium-containing abrasive, wherein preferably the calcium-containing abrasive is selected from the group consisting of calcium carbonate, calcium glycerophosphate, dicalcium phosphate, tricalcium phosphate, calcium orthophosphate, calcium metaphosphate, calcium polyphosphate, calcium oxyapatite, sodium carbonate, and combinations thereof. Preferably, the composition comprises from 27% to 47%, more preferably from 27% to 37%, even more preferably from 28% to 34%, yet even more preferably from 29% to 33%, by weight of the composition, alternatively combinations thereof, of a calcium-containing abrasive.

Preferably, the calcium-containing abrasive is calcium carbonate. More preferably, the calcium-containing abrasive is selected from the group consisting of fine ground natural chalk, ground calcium carbonate, precipitated calcium carbonate, and combinations thereof.

Fine ground natural chalk (FGNC) is one of the more preferred calcium-containing abrasives useful in the present invention. It is obtained from limestone or marble. FGNC may also be modified chemically or physically by coating during milling or after milling by heat treatment. Typical coating materials include magnesium stearate or oleate. The morphology of FGNC may also be modified during the milling process by using different milling techniques, for example, ball milling, air-classifier milling or spiral jet milling. One example of natural chalk is described in WO 03/030850 having a medium particle size of 1 to 15 μm and a BET surface area of 0.5 to 3 m²/g. The natural calcium carbonate may have a particle size of 325 to 800 mesh, alternatively a mess selected from 325, 400 600, 800, or combinations thereof; alternatively, the particle size is from 0.1 to 30 microns, or from 0.1 to 20 microns, or from 5 to 20 microns. In one embodiment, the composition comprises from 0% to 5%, preferably 0% to 3%, more preferably 0% to 1%, by weight of the composition, of a silicate; yet more preferably the composition is substantially free silicate.

Fluoride Ion Source

The compositions may include an effective amount of an anti-caries agent. In one embodiment, the anti-caries agent is a fluoride ion source. The fluoride ion may be present in an amount sufficient to give a fluoride ion concentration in the composition at 25° C., and/or in one embodiment can be used at levels of from 0.0025% to 5% by weight of the composition, alternatively from 0.005% to 2.0% by weight of the composition, to provide anti-caries effectiveness. Representative fluoride ion sources include: stannous fluoride, sodium fluoride, potassium fluoride, amine fluoride, sodium monofluorophosphate, and zinc fluoride. In one embodiment the dentifrice composition contains a fluoride source selected from stannous fluoride, sodium fluoride, and mixtures thereof. In one embodiment, the fluoride ion source is sodium monofluorophosphate, and wherein the composition comprises 0.0025% to 2%, by weight of the composition, of the sodium monofluorophosphate, alternatively from 0.5% to 1.5%, alternatively from 0.6% to 1.7%, alternatively combinations thereof. In another embodiment, the composition comprises from 0.0025% to 2%, by weight of the composition, of a fluoride ion source. In one example, the dentifrice compositions of the present invention may have a dual fluoride ion source, specifically sodium monofluorophosphate and an alkaline metal fluoride. Such an approach may provide an improvement in mean fluoride update.

Basic Amino Acid

The dentifrice compositions of the present invention comprise a basic amino acid in free or salt form. The basic amino acids which can be used in the compositions herein include not only naturally occurring basic amino acids, such as arginine, lysine, and histidine, but also any basic amino acids having a carboxyl group and an amino group in the molecule, which are water-soluble and provide an aqueous solution with a pH of 7 or greater. Accordingly, basic amino acids may include arginine, lysine, citrulline, ornithine, creatine, histidine, diaminobutanoic acid, diaminoproprionic acid, salts thereof, or combinations thereof. Preferably the basic amino acids are selected from arginine, citrulline, and ornithine, and combinations thereof; more preferably the basic amino acid is arginine (e.g., 1-arginine, or a salt thereof). Suitable salts include salts known in the art to be pharmaceutically acceptable salts considered to be physiologically acceptable in the amounts and concentrations provided. Non-limiting examples of such salts include those derived from alkali metals such as potassium and sodium or alkaline earth metals such as calcium and magnesium. Preferably the dentifrice compositions of the present invention comprise from 0.0025% to less than 7%, by weight of the composition, of a basic amino acid in free or salt form, wherein the weight of the basic amino acid being calculated as free base form. More preferably the compositions comprises from 0.1 to less than 7%, yet more preferably from 0.3 to less than 5%, alternatively from 0.5% to 3%, by weight of the composition, of the basic amino acid in free or salt form, preferably wherein the basic amino acid in free or salt form is arginine bicarbonate. Preferably the dentifrice compositions of the present invention comprise both arginine bicarbonate and calcium carbonate for inter alia reducing or preventing dentinal hypersensitivity.

pH

The pH of the dentifrice composition may be greater than pH 7.8, preferably greater than pH 8, more preferably from greater than pH 8.0 to pH 11. Preferably, the pH is greater than 8.1, more preferably the pH is greater than pH 8.5, even more preferably the pH is greater than pH 9, alternatively the pH is from pH 9.0 to pH 10.5, alternatively from pH 9 to pH 10. The relatively high pH of the present inventive composition is for fluoride stability. Without wishing to be bound theory, at below pH 8 calcium ion may bind with the fluoride. Thus, it is desirable to have the dentifrice composition have a greater than pH 8.0 to maximize the stability of the fluoride ion source. A method for assessing pH of dentifrice is described is provided the analytical methods section provided below. For purposes of clarification, although the analytical method describes testing the dentifrice composition when freshly prepared, for purposes of claiming the present invention, the pH may be taken at anytime during the product's reasonable lifecycle (including but not limited to the time the product is purchased from a store and brought to the consumer's home).

pH Modifying Agent

The dentifrice compositions herein may include an effective amount of a pH modifying agent, alternatively wherein the pH modifying agent is a pH buffering agent. The pH modifying agents, as used herein, refer to agents that can be used to adjust the pH of the dentifrice compositions to the above-identified pH range. The pH modifying agents may include alkali metal hydroxides, ammonium hydroxide, organic ammonium compounds, carbonates, sesquicarbonates, borates, silicates, phosphates, imidazole, and mixtures thereof. Specific pH agents include monosodium phosphate (monobasic sodium phosphate or “MSP”), trisodium phosphate (sodium phosphate tribasic dodecahydrate or “TSP”), sodium benzoate, benzoic acid, sodium hydroxide, potassium hydroxide, alkali metal carbonate salts, sodium carbonate, imidazole, pyrophosphate salts, sodium gluconate, lactic acid, sodium lactate, citric acid, sodium citrate, phosphoric acid. In one embodiment, 0.01% to 3%, preferably from 0.1% to 1%, by weight of the composition, of TSP, and 0.001% to 2%, preferably from 0.01% to 0.3%, by weight of the composition, of monosodium phosphate is used. Without wishing to be bound by theory, TSP and monosodium phosphate may also have calcium ion chelating activity and therefore provide some monofluorophosphate stabilization (in those formulations containing monofluorophosphate).

A method for assessing pH of dentifrice is described. The pH is measured by a pH Meter with Automatic Temperature Compensating (ATC) probe. The pH Meter is capable of reading to 0.001 pH unit. The pH electrode may be selected from one of the following (i) Orion Ross Sure-Flow combination: Glass body—VWR #34104-834/Orion #8172BN or VWR#10010-772/Orion #8172BNWP; Epoxy body—VWR #34104-830/Orion #8165BN or VWR#10010-770/Orion #8165BNWP; Semi-micro, epoxy body—VWR #34104-837/Orion #8175BN or VWR#10010-774/Orion #3175BNWP; or (ii) Orion PerpHect combination: VWR #34104-843/Orion #8203BN semi-micro, glass body; or (iii) suitable equivalent. The automatic temperature compensating probe is Fisher Scientific, Cat #13-620-16.

A 25% by weight slurry of dentifrice is prepared with deionized water, and thereafter is centrifuged for 10 minutes at 15000 rotations-per-minute using a SORVALL RC 28S centrifuge and SS-34 rotor (or equivalent gravitational force, at 24149 g force). The pH is assessed in supernatant after one minute or the taking reading is stabilized. After each pH assessment, the electrode is washed with deionized water. Any excess water is wiped with a laboratory grade tissue. When not in issue, the electrode is kept immersed in a pH 7 buffer solution or an appropriate electrode storage solution.

Low Level or Free of Humectants

The compositions herein contains relatively low amount, or even be substantially free or free, of humectants. Without wishing to be bound by theory, the presence of humectant (e.g., sorbitol/glyercol) may have a negative role in fluoride update in dental plaque in the high water and high carbonate containing dentifrice formulations of the present invention. Reduced levels of sorbitol/glycerol in these dentifrice compositions provide superior fluoride uptake results. Preferably the dentifrice compositions of the present invention comprise from 0% to 10%, by weight of the composition, of a humectant, wherein the humectant is selected from soribitol, glycerol, and combination thereof; more preferably the composition contain from 0% to 5%, yet more preferably 0% to 3%, yet still more preferably 0% to 1%, by weight of the composition of said humectant; alternatively, the composition is substantially free of the subject humectant.

More preferably the dentifrice compositions of the present invention comprise from 0% to 10%, by weight of the composition, of a humectant (as defined herein below); more preferably the composition contain from 0% to 5%, yet more preferably 0% to 3%, yet still more preferably 0% to 1%, by weight of the composition of said humectant; alternatively, the composition is substantially free of the subject humectant. The term “humectant,” for the purposes of present invention, include edible polyhydric alcohols such as glycerin, sorbitol, xylitol, butylene glycol, propylene glycol, and combinations thereof. In one embodiment, the humectant is a polyol, preferably wherein the polyol is selected from sorbitol, glycerin, and combinations thereof. In yet another embodiment, the humectant is sorbitol. A potential advantage of having a dentifrice composition that contain low levels of humectant (i.e., at or less than 10 wt %), without wishing to be bound by theory, is those dentifrice compositions that are free humectants such as glyercol or sorbitol may provide better fluoride uptake as compared to those compositions having the high levels of such humectants. In one example, the dentifrice compositions of the present invention comprise from 0% to 5%, preferably 0% to 3%, more preferably 0% to 1%, by weight of the composition, of glycerin, sorbitol, or combinations thereof; yet more preferably the composition is substantially free of both glycerin and sorbitol.

Thickening System

The dentifrice compositions of the present invention may comprise a thickening system. Preferably the dentifrice composition comprises from 0.5% to 4%, preferably from 0.8% to 3.5%, more preferably from 1% to 3%, yet still more preferably from 1.3% to 2.6%, by weight of the composition, of the thickening system. More preferably the thickening system comprises a thickening polymer, a thickening silica, or a combination thereof. Yet more preferably, when the thickening system comprises a thickening polymer, the thickening polymer is selected from a carboxymethyl cellulose, a linear sulfated polysaccharide, a natural gum, and combination thereof. Yet still more preferably, when the thickening system comprises a thickening polymer, the thickening polymer is selected from the group consisting of: (a) 0.01% to 3% of a carboxymethyl cellulose (“CMC”) by weight of the composition, preferably 0.1% to 2.5%, more preferably 0.2% to 1.5%, by weight of the composition, of CMC; (b) 0.01% to 2.5%, preferably 0.05% to 2%, more preferably 0.1% to 1.5%, by weight of the composition, of a linear sulfated polysaccharide, preferably wherein the linear sulfated polysaccharide is a carrageenan; (c) 0.01% to 7%, preferably 0.1% to 4%, more preferably from 0.1% to 2%, yet more preferably from 0.2% to 1.8%, by weight of the composition, of a natural gum; (d) combinations thereof. Preferably when the thickening system comprises a thickening silica, the thickening silica is from 0.01% to 10%, more preferably from 0.1% to 9%, yet more preferably 1% to 8% by weight of the composition.

Preferably the linear sulfated polysaccharide is a carrageenan (also known as carrageenin). Examples of carrageenan include Kappa-carrageenan, Iota-carrageenan, Lambda-carrageenan, and combinations thereof.

In one example the thickening silica is obtained from sodium silicate solution by destabilizing with acid as to yield very fine particles. One commercially available example is ZEODENT® branded silicas from Huber Engineered Materials (e.g., ZEODENT® 103, 124, 113 115, 163, 165, 167).

In one example the CMC is prepared from cellulose by treatment with alkali and monochloro-acetic acid or its sodium salt. Different varieties are commercially characterized by viscosity. One commercially available example is Aqualon™ branded CMC from Ashland Special Ingredients (e.g., Aqualon™ 7 H3SF; Aqualon™ 9 M3SF Aqualon™ TM9A; Aqualon™ TM12A).

Preferably a natural gum is selected from the group consisting of gum karaya, gum arabic (also known as acacia gum), gum tragacanth, xanthan gum, and combination thereof. More preferably the natural gum is xanthan gum. Xanthan gum is a polysaccharide secreted by the bacterium Xanthomonas camestris. Generally, xanthan gum is composed of a pentasaccharide repeat units, comprising glucose, mannose, and glucuronic acid in a molar ratio of 2:2:1, respectively. The chemical formula (of the monomer) is C₃₅H₄₉O₂₉. In one example, the xanthan gum is from CP Kelco Inc (Okmulgee, US).

Viscosity

Preferably the dentifrice compositions of the present invention have a viscosity range from 150,000 centipoise to 850,000 centipoise (“cP”). A method for assessing viscosity is described. The viscometer is Brookfield® viscometer, Model DV-I Prime with a Brookfield “Helipath” stand. The viscometer is placed on the Helipath stand and leveled via spirit levels. The E spindle is attached, and the viscometer is set to 2.5 RPM. Detach the spindle, zero the viscometer and install the E spindle. Then, lower the spindle until the crosspiece is partially submerged in the paste before starting the measurement. Simultaneously turn on the power switch on the viscometer and the helipath to start rotation of the spindle downward. Set a timer for 48 seconds and turn the timer on at the same time as the motor and helipath. Take a reading after the 48 seconds. The reading is in cP.

PEG

The compositions of the present invention may optionally comprise polyethylene glycol (PEG), of various weight percentages of the composition as well as various ranges of average molecular weights. In one aspect of the invention, the compositions have from 0.01% to 8%, preferably from 0.1% to 5%, more preferably from 0.2% to 4.8%, yet more preferably from 0.3% to 4.2%, yet still more preferably from 0.5% to 4%, by weight of the composition, of PEG. In another aspect of the invention, the PEG is one having a range of average molecular weight from 100 Daltons to 1600 Daltons, preferably from 200 to 1000, alternatively from 400 to 800, alternatively from 500 to 700 Daltons, alternatively combinations thereof. PEG is a water soluble linear polymer formed by the addition reaction of ethylene oxide to an ethylene glycol equivalent having the general formula is: H—(OCH₂CH₂)_(n)—OH. One supplier of PEG is Dow Chemical Company under the brandname of CARBOWAX™. Without wishing to be bound by theory, having some PEG in the dentifrice composition may help with physical stability.

Sweetener

The oral care compositions herein may include a sweetening agent. These include sweetening agents may include saccharin, dextrose, sucrose, lactose, maltose, levulose, aspartame, sodium cyclamate, D-tryptophan, dihydrochalcones, acesulfame, sucralose, neotame, and mixtures thereof. Sweetening agents are generally used in oral compositions at levels of from 0.005% to 5%, by weight of the composition, alternatively 0.01% to 1%, alternatively from 0.1% to 0.5%, alternatively combinations thereof.

Anti-Calculus Agent

The dentifrice compositions may include an effective amount of an anti-calculus agent, which in one embodiment may be present from 0.05% to 50%, by weight of the composition, alternatively from 0.05% to 25%, alternatively from 0.1% to 15% by weight of the composition. Non-limiting examples include those described in US 2011/0104081 A1 at paragraph 64, and those described in US 2012/0014883 A1 at paragraphs 63 to 68, as well as the references cited therein. One example is a pyrophosphate salt as a source of pyrophosphate ion. In one embodiment, the composition comprises tetrasodium pyrophosphate (TSPP) or disodium pyrophosphate or combinations thereof, preferably 0.01% to 2%, more preferably from 0.1% to 1%, by weight of the composition, of the pyrophosphate salt. Without wishing to be bound by theory, TSPP may provide not only calcium chelating thereby mitigating plaque formation, but also may also provide the additional benefit of monofluorophosphate stabilization (in those formulations containing monofluorophosphate).

Surfactant

The dentifrice compositions herein may include a surfactant. The surfactant may be selected from anionic, nonionic, amphoteric, zwitterionic, cationic surfactants, or mixtures thereof. The composition may include a surfactant at a level of from 0.1% to 10%, from 0.025% to 9%, from 0.05% to 5%, from 0.1% to 2.5%, from 0.5% to 2%, or from 0.1% to 1% by weight of the total composition. Non-limiting examples of anionic surfactants may include those described at US 2012/0082630 A1 at paragraphs 32, 33, 34, and 35. Non-limiting examples of zwitterionic or amphoteric surfactants may include those described at US 2012/0082630 A1 at paragraph 36; cationic surfactants may include those described at paragraphs 37 of the reference; and nonionic surfactants may include those described at paragraph 38 of the reference. In one embodiment the composition comprises 0.1% to 5%, preferably 0.1% to 3%, alternatively from 0.3% to 3%, alternatively from 1.2% to 2.4%, alternatively from 1.2% to 1.8%, alternatively from 1.5% to 1.8%, by weight of the composition, alternatively combinations thereof, of the anionic surfactant sodium lauryl sulfate (SLS).

Colorant The compositions herein may include a colorant. Titanium dioxide is one example of a colorant. Titanium dioxide is a white powder which adds opacity to the compositions. Titanium dioxide generally can comprise from 0.25% to 5%, by weight of the composition.

Flavorant

The compositions herein may include from 0.001% to 5%, alternatively from 0.01% to 4%, alternatively from 0.1% to 3%, alternatively from 0.5% to 2%, alternatively 1% to 1.5%, alternatively 0.5% to 1%, by weight of the composition, alternatively combinations thereof, of a flavorant composition. The term flavorant composition is used in the broadest sense to include flavor ingredients, or sensates, or sensate agents, or combinations thereof. Flavor ingredients may include those described in US 2012/0082630 A1 at paragraph 39; and sensates and sensate ingredients may include those described at paragraphs 40-45, incorporated herein by reference. Excluded from the definition of flavorant composition is “sweetener” (as described above).

Examples

Improved Fluoride Uptake in Dual Fluoride Source/High Water/High Carbonate Dentifrice Compositions

Data is provided to demonstrate the superiority of inventive Example 1 in fluoride uptake. The sodium monofluorophosphate, nil polyol humectant, at pH 9.5 dentifrice formulation of example 1 provides better results as compared to comparative examples 2 and 3, as well as control compositions that include marketed toothpaste products. Table 1 below details the components of the five compositions on a weight percentage (wt %) basis. Methods are described including determining Mean Fluoride Uptake. Lastly, data is presented in Table 2.

Compositional Components

TABLE 1 Compositional components of inventive example 1, and comparative examples 2, 3, and 4 are provided. Ex 1 Ex 2 Ex 3 Ex 4 Inventive Comparative Comparative Comparative Components: (Arginine, nil (Arginine, + (Nil arginine, (Nil arginine, + (Wt %) humectant) sorbitol) nil humectant) sorbitol) Water 57.75 32.75 58.75 33.75 CaCO₃ 32 32 32 32 Sorbitol 0 25 0 25 Arginine Bicarbonate 1 1 0 0 Sodium Mono- 1.1 1.1 1.1 1.1 fluorophosphate Sodium Caboxy- 0.9 0.9 0.9 0.9 methyl Cellulose Carrageenan 1.2 1.2 1.2 1.2 Thickener Silica 2.6 2.6 2.6 2.6 Sodium Lauryl 1 1 1 1 Sulfate Tetra Sodium 0.6 0.6 0.6 0.6 Pyrophosphate Flavor 1 1 1 1 Sodium 0.1 0.1 0.1 0.1 Monophosphate Sodium Triphosphate 0.4 0.4 0.4 0.4 Sodium Saccharine 0.25 0.25 0.25 0.25 Total: 100 100 100 100

Referring to Table 1, the inventive composition (Ex 1) notably contains: sodium monofluorophosphate; Arginine bicarbonate (1 wt %); nil polyol humectant (i.e., nil glycerin and nil sorbitol); and is at pH 9.5. Example 1 also has a relatively high level of water (57.75 wt %) and calcium carbonate (32 wt %). Comparative example 2 notably contains a high level of the polyol humectant sorbitol (25 wt %). The only component difference between example 1 and 2, is that example 2 replaces the water of example 1 with sorbitol. Comparative example 3 is the same as example 1 but notably does not contain arginine bicarbonate. Lastly, comparative example 4 notably also does not contain arginine bicarbonate but contains sorbitol (25 wt %).

Analytical Methods

The method for assessing “Mean Fluoride Uptake” is described. Glass rods (Tianjin Hope Biotech Co., Ltd.) are polished with fine wet/dry #600 sandpaper on lathe. Rods are weighed on a four decimal place balance (Sartorius, BP210 S). Then the rods are mounted on stainless steel racks using rubber o-rings to secure using spacers to control depth.

Culture medium is prepared and autoclaved with 60 g TSB (Becton, Dickinson and Company), 60G sucrose (Becton, Dickinson and Company), and 2000 ml DI water. 180 ml pooled fresh saliva is mixed with 120 ml Sucrose/TSB solution to form a culture mixture. 7 ml of this mixture is pipetted with repeater pipette into 16×100 mm borosilicate tubes placed in a dosing rack. Glass rod rack and dosing solution rack are placed in incubator overnight with dipping motor on. The mix and growth steps are repeated in the morning and afternoon, and then are incubated overnight. The culture mixture is changed for a total of five times.

Dentifrice treatment is prepared by thoroughly mixing 15 g of dentifrice with 45 g of fresh pooled saliva (i.e., a 1:3 weight ratio). Plaque rods for are dipped for two minutes in ten ml of slurry, and then the rods are rinsed for ten seconds in DI water. This is repeated for a total of two rinses. The treatment is repeated for two minutes and rinsed twice.

A small spatula is sterilized with 70% alcohol. Plaque rods are carefully inserted into sterile labeled, pre-weighed 1.5 ml Eppendorf™ tubes and wiped on the sides of the tube. The plaque is dried in the Eppendorf™ tubes in 60° C. incubator overnight until dry. The dried plaque is weighed in the Eppendorf™ tubes on a four decimal place balance. The net plaque weight is calculated. 10 ul of 1.0 M perchloric acid is added to the Eppendorf™ tube. The tubes incubate at room temperature in the hood overnight. In the morning, 100 ml 1.0M NaOH is added to increase the pH to 5.0.

Fluoride concentration is determined from a calibration curve obtained on the same day as the analysis. This standard curve is made using an ion selective electrode (Orion, Model 9609BNWP) and previously made fluoride standards. These standards are made using 1.0 mL fluoride standard and 1.0 mL TISAB II (1:1). The following parts per million (“ppm”) F standards atre used: 250, 100, 50, 25, 10, 5, 2.5, 1.0, 0.5, 0.1, 0.05, 0.025 and 0.01 ppm F. The equation for log ppm F is then obtained by graphing log ppm F vs. Rel mV readings for each of the above standards and obtaining a linear fit line and equation. In the Eppendorf™ tube, 200 ul of TISAB II buffer is added and allowed to sit for 10 minutes to buffer pH; thereafter, fluoride is measured with an ion selective electrode, calibrated against the standard curve. The data is provided in Table 2 below.

Data

TABLE 2 Mean Fluoride Uptake in Plaque among various dentifrice products/formulations Plaque Mean Arginine Fluoride Bicarbonate Uptake ± Product¹ pH Humectant (wt %) (SEM) Statistic Ex 1 9.5 Nil 1.0 640 B Ex 2 9.4 Sorbitol (25 wt %) 1.0 536 C Ex 3 9.5 Nil 0 985 A Ex 4 9.4 Sorbitol (25 wt %) 0 584 B A² 9.0 Sorbitol~30 wt % ~8 447 D B³ 9.1 Sorbitol~30 wt % ~1.5 363 D ¹Fluoride Source (ppm or parts per million) is 1450 total fluoride (1.1 wt % sodium mono-fluorophosphate) for all products tested. ²Control A: COLGATE Pro-Argin (LOT: EXP0515(L)3128^(TH)11J1); containing around 8% w/w Arginine Bicarbonate ³Control B: COLGATE Maximum Acid-Neutralizer (EXP1115(L)3307CN11V4) containing around 1.5% w/w Arginine Bicarbonate

Table 2 summarizes the results obtained from measuring the Plaque Mean Fluoride Uptake across the identified examples and controls. The first column identifies the product name Composition components for Examples 1-4 are provided in Table 1 above. Notably Example 1 is inventive. Results for commercial products A and B are also provided. The second column provides the pH of the composition. The pH for all samples tested is from 9.0 to 9.5. The third column identifies the humectant and amount thereof, if any. Examples 1 and 3 do not contain any humectant, whereas Example 2, 4, and Products A and B contain sorbitol (as the humectant). The fourth column identifies the amount of arginine bicarbonate, if any. Examples 1 and 2 contain 1 wt % where as Products A and B contains about 8 wt % and 1.5 wt %, respectively. The fifth column provides the Plaque Mean Fluoride Uptake. The method is described above. Lastly, the final column labeled as “Statistic” designates whether any tested product is A, B, C, or D (with A as the highest performing sample and D as the lowest performing sample with respect to fluoride Uptake). A Gate-keeper Tukey statistical pair-comparison analysis method is used to group treatments and assess the relevant Statistic.

Example 1 is the inventive dentifrice composition notably containing arginine bicarbonate and nil humectant. Example 1 provides relatively high level of plaque mean fluoride update at 640. Comparative example 3 provides the best comparative results of plaque mean fluoride uptake at 985, but example 3 does not include any arginine bicarbonate. Although example 1 is not as high as control example 3 in fluoride update, it contains arginine bicarbonate (1 wt %) whereas example 3 does not. Accordingly, Example 3 fails to provide any of the benefits associated arginine bicarbonate.

Comparative example 2 contains arginine bicarbonate but also humectant. Example 2 exhibits relatively poor fluoride uptake (536) compared to the inventive example 1. Without wishing to be bound by theory, the presence of humectant in the arginine bicarbonate containing dentifrice compositions defined herein appears to have a negative influence on fluoride uptake.

Comparative example 4 exhibits better fluoride uptake (584) as compared to example 2, but notably example 4 does not include any arginine bicarbonate. Both examples 2 and 4 contain humectant (i.e., 25 wt % sorbitol). Without wishing to be bound by theory, the defined dentifrice formulation that contains humectant and arginine has negative impact on fluoride uptake since example 4, by not having arginine, has better fluoride uptake than example 2.

In view of these examples and data, the inventive formulation with arginine but without humectant has relatively high fluoride uptake but ostensibly provides benefits associated arginine bicarbonate.

Two commercial products are also provided (i.e., Products A and B). These products have comparatively the same fluoride source of sodium mono-fluorophosphate and total level of fluoride (i.e., at 1450 ppm). Both products A and B have humectant (about 30 wt % sorbitol) but also contain arginine bicarbonate at 8 wt % and about 1.5 wt %, respectively. The fluoride uptake is the poorest for Products A and B from samples tested.

One aspect of the invention provides for a use of any dentifrice composition according to the present invention to provide a Mean Fluoride Uptake (as described herein) greater than 550 ppm, preferably greater than 600 ppm, more preferably greater than 625 ppm.

The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as “40 mm” is intended to mean “about 40 mm.”

Every document cited herein, including any cross referenced or related patent or application and any patent application or patent to which this application claims priority or benefit thereof, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests or discloses any such invention. Further, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.

While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope of this invention. 

What is claimed is:
 1. A dentifrice composition comprising: (a) 45% to 75%, by weight of the composition, of water; (b) 25% to 50%, by weight of the composition, of a calcium-containing abrasive; (c) 0.0025% to 2%, by weight of the composition, of a fluoride ion source; (d) 0.0025% to less than 7%, by weight of the composition, of a basic amino acid in free or salt form; (e) 0% to 10%, by weight of the composition, of a humectant, wherein the humectant is selected from sorbitol, glycerol, and a combination thereof; and wherein said composition has a pH greater than 7.8.
 2. The dentifrice composition of claim 1, comprising from 0% to 5%, by weight of the composition, humectant.
 3. The dentifrice composition of claim 1, wherein the composition is substantially free of humectant.
 4. The dentifrice composition of claim 1, wherein the composition comprises a humectant and the humectant is a polyol humectant.
 5. The dentifrice composition of claim 1, wherein the composition comprises from 0.3% to less than 5%, by weight of the composition, of the basic amino acid in free or salt form, wherein the weight of the basic amino acid being calculated as free base form.
 6. The dentifrice composition of claim 5, wherein a basic amino acid from the basic amino acid in free or salt form is selected from the group consisting of arginine, lysine, citrulline, ornithine, creatine, histidine, diaminobutanoic acid, diaminoproprionic acid and combinations thereof.
 7. The dentifrice composition of claim 5, wherein the basic amino acid from the basic amino acid in free or salt form is selected from the group consisting of arginine, citrulline, and ornithine.
 8. The dentifrice composition of claim 7, wherein the basic amino acid from the basic amino acid in free or salt form comprises arginine.
 9. The dentifrice composition of claim 8, wherein the basic amino acid from the basic amino acid in free or salt form comprises arginine bicarbonate.
 10. The dentifrice composition of claim 1, wherein the composition comprises from 0.2% to 1.5% fluoride ion source and wherein the fluoride ion source comprises sodium monofluorophosphate.
 11. The dentifrice composition of claim 1, wherein the composition comprises from 27% to 37% calcium-containing abrasive and wherein the calcium-containing abrasive comprises calcium carbonate.
 12. The dentifrice composition of claim 1, wherein the pH is greater than 8.5.
 13. The dentifrice composition of claim 12, wherein the pH is from 8.5 to 10.5.
 14. The dentifrice composition of claim 1, wherein the composition comprises from 50% to 60%, by weight of the composition, of water.
 15. The dentifrice composition of claim 1, wherein the composition comprises from 0% to 5%, by weight of the composition, of a silicate.
 16. The dentifrice composition of claim 15, wherein the composition is substantially free of silicate.
 17. The dentifrice composition according to claim 1, further comprising a thickening system, wherein the thickening system is selected from the group consisting of a thickening polymer, a thickening silica, or combinations thereof.
 18. The dentifrice composition according to claim 17, wherein the thickening system comprises a thickening polymer wherein the thickening polymer is selected from the group consisting of carboxymethyl cellulose, linear sulfated polysaccharide, natural gum, and combinations thereof.
 19. A dentifrice composition comprising: (a) 45% to 75%, by weight of the composition, of water; (b) 25% to 50%, by weight of the composition, of a calcium carbonate; (c) 0.1% to 2%, by weight of the composition, of a sodium monofluorophosphate; (d) 0.1% to less than 7%, by weight of the composition, of arginine bicarbonate; (e) 0% to 5%, by weight of the composition, of a humectant; wherein said composition has pH from 8.5 to 10.5; and said composition is a single phase composition. 